A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14834658



Internal ID3626170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:87303757..87446217hg38UCSC Ensembl
chr13:87956012..88098472hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg38142461
hg19142461
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633039
Supporting Variants
SamplesHG03225
Known GenesMIR4500HG
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14834658
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer